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Barley Tortillas Study in Healthy Volunteers

Not Applicable
Completed
Conditions
Healthy
Interventions
Dietary Supplement: food product
Registration Number
NCT00831285
Lead Sponsor
University of Manitoba
Brief Summary

The variation in starch and fibre composition of prepared barley tortillas will have a significant effect on glycemic response.

Detailed Description

Specifically, we wish to examine the glycemic response of barley tortillas containing different ratios of amylose and amylopectin and different amounts of soluble and insoluble fibre with an appropriate control during acute phase testing in healthy volunteers. Possible relationships between composition of the barley tortillas and the degree of physiological response will also be investigated as the secondary objective.

Recruitment & Eligibility

Status
COMPLETED
Sex
All
Target Recruitment
12
Inclusion Criteria
  • male or female age 18 to 40 years
  • normal glycated hemoglobin of <6%
  • BMI of 20 to 30
  • must read the consent form
  • must comply with the protocol requirements
Exclusion Criteria
  • allergies to barley flour
  • presence of chronic conditions such as cardiovascular disease, hypertension, disorders affecting the gastrointestinal tract, thyroid disease, and requiring medication for these conditions
  • requiring medication for glycemic control
  • consumption of supplements which have an effect on blood glucose response

Study & Design

Study Type
INTERVENTIONAL
Study Design
PARALLEL
Arm && Interventions
GroupInterventionDescription
tortilla with high amylose flourfood product-
barley tortilla with low amylose flour and low soluble fibrefood product-
barley tortilla with low amylose flourfood product-
barley tortilla with low amylose flour and soluble fibrefood product-
barley tortilla with low amylose flour and insoluble fibrefood product-
glucosefood product-
Primary Outcome Measures
NameTimeMethod
Calculation of area under the curve for glucose and insulin6 weeks
Secondary Outcome Measures
NameTimeMethod
comparison of food groups using ANOVA6 weeks
measurement of incretins6 weeks

Trial Locations

Locations (1)

St. Boniface General Hospital Research Centre

🇨🇦

Winnipeg, Manitoba, Canada

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